US2165090A - Resinous compositions and capacitors containing the same - Google Patents
Resinous compositions and capacitors containing the same Download PDFInfo
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- US2165090A US2165090A US69405A US6940536A US2165090A US 2165090 A US2165090 A US 2165090A US 69405 A US69405 A US 69405A US 6940536 A US6940536 A US 6940536A US 2165090 A US2165090 A US 2165090A
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- 239000000203 mixture Substances 0.000 title description 35
- 239000003990 capacitor Substances 0.000 title description 21
- 239000000047 product Substances 0.000 description 31
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 28
- 239000002253 acid Substances 0.000 description 20
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 19
- ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 description 18
- 238000010438 heat treatment Methods 0.000 description 14
- 239000004310 lactic acid Substances 0.000 description 12
- 235000014655 lactic acid Nutrition 0.000 description 12
- 229960000448 lactic acid Drugs 0.000 description 12
- 239000003792 electrolyte Substances 0.000 description 11
- 150000001408 amides Chemical class 0.000 description 8
- 229910021529 ammonia Inorganic materials 0.000 description 8
- 150000003863 ammonium salts Chemical class 0.000 description 8
- 239000007788 liquid Substances 0.000 description 8
- 125000006850 spacer group Chemical group 0.000 description 7
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 6
- SXQFCVDSOLSHOQ-UHFFFAOYSA-N lactamide Chemical compound CC(O)C(N)=O SXQFCVDSOLSHOQ-UHFFFAOYSA-N 0.000 description 6
- 239000007787 solid Substances 0.000 description 6
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 5
- 239000004327 boric acid Substances 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 239000004615 ingredient Substances 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 239000004251 Ammonium lactate Substances 0.000 description 3
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- 229940059265 ammonium lactate Drugs 0.000 description 3
- 235000019286 ammonium lactate Nutrition 0.000 description 3
- RZOBLYBZQXQGFY-HSHFZTNMSA-N azanium;(2r)-2-hydroxypropanoate Chemical compound [NH4+].C[C@@H](O)C([O-])=O RZOBLYBZQXQGFY-HSHFZTNMSA-N 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 239000011888 foil Substances 0.000 description 3
- 238000005470 impregnation Methods 0.000 description 3
- 229920006395 saturated elastomer Polymers 0.000 description 3
- WYXIGTJNYDDFFH-UHFFFAOYSA-Q triazanium;borate Chemical compound [NH4+].[NH4+].[NH4+].[O-]B([O-])[O-] WYXIGTJNYDDFFH-UHFFFAOYSA-Q 0.000 description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- -1 aliphatic hydroxy acid Chemical class 0.000 description 2
- 150000003857 carboxamides Chemical class 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 150000002596 lactones Chemical class 0.000 description 2
- 239000012262 resinous product Substances 0.000 description 2
- KVZLHPXEUGJPAH-UHFFFAOYSA-N 2-oxidanylpropanoic acid Chemical compound CC(O)C(O)=O.CC(O)C(O)=O KVZLHPXEUGJPAH-UHFFFAOYSA-N 0.000 description 1
- SJZRECIVHVDYJC-UHFFFAOYSA-N 4-hydroxybutyric acid Chemical compound OCCCC(O)=O SJZRECIVHVDYJC-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000001447 alkali salts Chemical class 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 150000003868 ammonium compounds Chemical class 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- NTBYNMBEYCCFPS-UHFFFAOYSA-N azane boric acid Chemical class N.N.N.OB(O)O NTBYNMBEYCCFPS-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 229960004275 glycolic acid Drugs 0.000 description 1
- 235000015110 jellies Nutrition 0.000 description 1
- 239000008274 jelly Substances 0.000 description 1
- 239000012263 liquid product Substances 0.000 description 1
- 230000002101 lytic effect Effects 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 239000006187 pill Substances 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 239000012056 semi-solid material Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000012265 solid product Substances 0.000 description 1
- 239000004071 soot Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 229940005605 valeric acid Drugs 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G9/00—Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
- H01G9/004—Details
- H01G9/022—Electrolytes; Absorbents
Definitions
- the present invention comprises new resinous compositions suitable for use as electrolytes in capacitors, or other electrolytic devices, and a method of preparing such compositions.
- Electrolytes embodying our invention are of a semi-solid, balsamic or resinous consistency. They comprise as an essential ingredient a pyrogenous product derived from a mixture of suitable monobasic, satll urated, hydroxy aliphatic acid and its ammonium salt. Such material when used as an electrolyte preferably is modified by the presence of an ionogen and a resistance-modifying agent, such as an amide.
- FIG. 1 shows in perspective a roll type of electric capacitor (shown partly unrolled) and Fig. 2 diagrammatically indicates a stack type of capacitor.
- This type of product is known by chemists as an inner ester, this term being used herein to designate a pyrogenous product derived by heating such acid to a temperature of at least about 120 C. for several hours.
- hydroxy aliphatic acids are:
- Glycollic acid or hydroxy acetic acid Lactic or alpha hydroxy propionic acid; Gamma hydroxy butyric acid; and Gamma oxy-valeric acid.
- Example 1 A mixture consisting by weight of 64% lactic 5 acid and 36% b6ric acid is caused to combine with ammonia, for example, by conducting ammonia into the mixture of acids until the product is a thin, clear liquid having a pH value of 4.9,
- the boric acid is converted into ammonium borate which, as is well known, functions as an ionogen.
- the product is heated at about 120 to 130 C. for about four hours until a pyrogenous product is produced which is a waxy solid at 0., while being a clear liquid at 90 C.
- This pyrogenous product appears to consist in part at least of a lactamide even though the heat conversion is not necessarily carried so far that complete conversion to lactamide occurs.
- lactamide will be used herein to include also equivalent compositions which are obtained by the thermal breakdown of the ammonium salts of equivalent monobasic hydroxy aliphatic acids.
- the resistance of the lactamide at 90 C. is of the order of 6600 ohms per centimeter cube.
- the resistance is too high for the use of the described lactamide composition in electro-- lytic capacitors, and hence it is modified for such use by a resistance-reducing agent.
- Formamide which is soluble in the composition is well suited to the purpose of reducing its resistivity. If by weight 25% of iormamide and 75% of lactamide composition are compounded or mixed at 100 C. (with agitation to produce homogeneity), the resulting product is characterized by a pH value of about 5 and a resistance at 90 C. of 221 ohms/cm and at 25 C. of 23,200 ohms/em
- other saturated aliphatic, monoprimary amides such as acetamide may be used as resistance-reducing addition agents.
- the product is a clear thin liquid and therefore is well adapted for the impregnation of the porous spaces of capacitor units, or for the surface coating of capacitor armatures to be used without spacers.
- the product is a clear, viscous or plastic, semi-solid material.
- a typical roll type of capacitor consisting of aluminum armatures I, 2 and having terminals 3, 4 of the elongated strip type. Between adjacent turns of the armatures are porous spacers 5, 5' which are adapted to be impregnated with an electroapplied to the terminal plates or armatures.
- the spacer may be omitted.
- a spacer may consist of a fabric, such as cheesecloth, or of paper.
- the spacer consists of paper, which may be .001" in thickness and be sufficiently absorbent to be capable of being impregnated by the electrolyte when the latter is heated to 90 C. to 100 C. or thereabouts. Although but one sheet of paper is shown between adjacent turns, two or three may be used.
- capacitor armatures G, i may be stacked superposed, instead of rolled, preferably with one or more interposed spacers, one of which is indicated at 8. Terminals 9, ID are The aluminum foil should be treated to form an oxygenous film thereon prior to assembling of the capacitor parts, preferably by electrolytic treatment as described in prior Clark and Koenig Patent No. 2,022,500, patented November 26, 1935.
- the impregnation of a capacitor unit consisting of aluminum foil armatures with or without spacers therebetween when properly assembled may be carried out by immersing the unit in an electrolyte composition made as herein described while the latter is heated to a temperature at which it is thinly liquid, for example 100 C.
- gas under pressure of about 100 lbs. per square inch is applied to insure penetration of the electrolyte into the interstices oi the unit.
- the impregnated capacitor may be cured in accordance with the usual methods, for example, by applying intermittent uni-directional voltage of alternating polarity followed by the application of intermittent alternating voltage of no volts-60 cycles.
- Capacitors thus fabricated have a power factor of approximately 7% at 25 C., the capacity being about one microfarad for nine square inches oi active foil surface.
- capacitors so fabricated are subjected to temperatures as th gh as 75 C. even for a period of several weeks, no deterioration occurs in the capacity characteristic and in fact an improvement may resilit.
- the pyrogenous product is'treated with ammonia gas until the pill value is about 6.8 to 7, the resulting product consists oi. a thin, clear liquid at 90 C. and solidifies to a clear yellow jelly at 25 C.
- the ammonia-treated product has a resistance at 90 C. of the order 125 to 150 ohms/cm and at 25 C. of the order of soot ohms/ch1 It will be observed that the treatment with ammonia reduces the resistance value.
- Example 3 In some cases it is desirable to mix the ingredients, namely, lactic acid, boric acid and formamide before being subjected to heat treatment.
- a mixture consisting by weight of 48% lactic acid, 27% boric acid and 25% formamide is treated with ammonia gas at a temperature of 75 to C. until the pH value is of the order of 7.0 to 7.5.
- the product is heated at a temperature within'the range of about 130 to 140 C. for approximately 3 to 4 hours, or until the resistance of the pyrogenous product has reached a value of about 137 ohms/cm at C.
- the pyrogenous product is characterized in general by the properties already described in connection with the foregoing examples.
- Example 4 the individual reagents may be prepared separately and then mixed thoroughly to obtain the desired electrolyte.
- lactic acid may be treated with ammonia thereby forming ammonium lactate which then is heated to form a semi-solid lactamidecontaining product.
- This pyrogenous composition is admixed with ammonium borate crystals and formamide in the proportions above indicated.
- the resulting product is heated to a temperature at which it is liquid and impregnation is carried out as above described.
- the amide which may consist oi. formamide, or a combination of amides such as acetamide and formamide, should not constitute more than 40% by weight of the total mixture. Itis also preferred in general that the lactic acid component of the final product should be at least as great as the amide component. In place of lactic acid, other aliphatic hydroxy acids may be used, such as heretofore indicated.
- ammonium borate salts of other oxygen-containing acids may be used as ionogens.
- ammonium or alkali salts sodium or potassium salts
- the ammonium or alkali salts sodium or potassium salts of phosphoric acid, tartaric acid, acetic acid or citric acid.
- a viscous, semi-solid impregnating composition for electrolytic capacitors having filmiorn'iing electrodes said impregnant including ammonium borate, a waxy solid product derived by heat treatment of ammoniated lactic acid, constituting a major ingredient and iormamide, constituting a minor ingredient, said composition being liquid at 90 C.
- the combination of film-forming electrodes and a composition comprising the combination of an ionogen, iormamide and a product derived by heating to a temperature of at least about 120 C. a mixture of an acid of said group consisting of alpha, gamma and delta monobasic, saturated hydroxy aliphatic acid and ammonium salt of an acid of said group.
- a composition comprising in combination a waxy product derived by heating ammoniated lactic acid to about 120 to C., an ionogen, and a resistance-reducing material.
- a composition comprising a mixture of a waxy product derived by heating lacticacid to at least about 120 C., an ionogen, and formamide in a quantity adequate to appreciably modify the electric resistivity of said mixture.
- a semi-solid balsamic materiai for use with film-forming electrodes comprising the combination of an ionogen, saturated, monoprimary organic amide and a waxy product derived by heating an ammoniated compound of lactic acid.
- An electric capacitor containing film-forming armatures and an electrolyte comprising the combintion of an ionogen, iormamide and a product derived by heating to a temperature of about 120 to 140 C. for several hours an ammoniated acid of the group consisting of alpha, gamma and delta monobasic, saturated hydroxy aliphatic acid.
- a composition of matter comprising the combination of .an ionogen, a saturated, monoprimary organic amide, and an inner ester derived by heating to a temperature of about 120 to 140 0., an ammoniated, saturated hydroxy aliphatic acid.
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Description
Jul 4, 1939.
F. M. CLARK ET AL 2,165,090
RESINOUS COMPOSITIONS AND CAPACITORS CONTAINING THE SAME Filed March 17, 1936 ngz.
Inventors: Frank M. Clark Palph Apuscetta,
Their tcorneu.
Patented July 4, 1939 UNITED STATES PATENT OFFICE RESINOUS COMPOSITIONS AND CAPACI- TORS CONTAINING THE SAME Application March 17, 1936, Serial No. 89,405
12 Claims.
The present invention comprises new resinous compositions suitable for use as electrolytes in capacitors, or other electrolytic devices, and a method of preparing such compositions.
. It is the object of our invention to provide electrolytes of improved physical and chemical characteristics which in particular will have a high degree of stability in the elevated range 01' temperatures to which capacitors are exposed under working conditions. Electrolytes embodying our invention are of a semi-solid, balsamic or resinous consistency. They comprise as an essential ingredient a pyrogenous product derived from a mixture of suitable monobasic, satll urated, hydroxy aliphatic acid and its ammonium salt. Such material when used as an electrolyte preferably is modified by the presence of an ionogen and a resistance-modifying agent, such as an amide.
In the accompanying drawing Fig. 1 shows in perspective a roll type of electric capacitor (shown partly unrolled) and Fig. 2 diagrammatically indicates a stack type of capacitor.
The alpha, gamma and delta monobasic, saturated hydroxy aliphatic acids when heated lose water with the formation of anhydrides, commonly classified as lactides or lactones, depend ing on the nature of the parent material which is used. This type of product is known by chemists as an inner ester, this term being used herein to designate a pyrogenous product derived by heating such acid to a temperature of at least about 120 C. for several hours. Illustrative of the type of materials which are included under the description hydroxy aliphatic acids are:
Glycollic acid or hydroxy acetic acid; Lactic or alpha hydroxy propionic acid; Gamma hydroxy butyric acid; and Gamma oxy-valeric acid.
In the preparation of our electrolyte of high thermal stability we subject to pyrogenous decomposition a mixture of the aliphatic hydroxy acid and its ammonium salt as will be later illustrated. We believe that as a result of the pyrogenous decomposition we produce a mixture of the lactlde or lactone type of compound (depending on the particular type of acid used) and the acid amide formed in accordance with known phenomena from the ammonium salt of the acid.
Of the possible pyrogenous products derived from a mixture of the hydroxy aliphatic acids and their ammonium salts, we prefer the product obtained from lactic acid (alpha hydroxy propionic acid) and ammonium lactate.
The following examples will further explain the novel features of our invention.
Example 1 A mixture consisting by weight of 64% lactic 5 acid and 36% b6ric acid is caused to combine with ammonia, for example, by conducting ammonia into the mixture of acids until the product is a thin, clear liquid having a pH value of 4.9,
'a resistance at 25 C. of 200 ohms per centimeter 10 cube. At 90 C. the resistance of the product is 9 ohms per centimeter cube. The boric acid is converted into ammonium borate which, as is well known, functions as an ionogen. The product is heated at about 120 to 130 C. for about four hours until a pyrogenous product is produced which is a waxy solid at 0., while being a clear liquid at 90 C. This pyrogenous product appears to consist in part at least of a lactamide even though the heat conversion is not necessarily carried so far that complete conversion to lactamide occurs. The term lactamide will be used herein to include also equivalent compositions which are obtained by the thermal breakdown of the ammonium salts of equivalent monobasic hydroxy aliphatic acids. The resistance of the lactamide at 90 C. is of the order of 6600 ohms per centimeter cube.
At 250 C. the resistance is too high for the use of the described lactamide composition in electro-- lytic capacitors, and hence it is modified for such use by a resistance-reducing agent. Formamide which is soluble in the composition is well suited to the purpose of reducing its resistivity. If by weight 25% of iormamide and 75% of lactamide composition are compounded or mixed at 100 C. (with agitation to produce homogeneity), the resulting product is characterized by a pH value of about 5 and a resistance at 90 C. of 221 ohms/cm and at 25 C. of 23,200 ohms/em As hereinafter indicated, other saturated aliphatic, monoprimary amides, such as acetamide may be used as resistance-reducing addition agents.
At 90 C. the product is a clear thin liquid and therefore is well adapted for the impregnation of the porous spaces of capacitor units, or for the surface coating of capacitor armatures to be used without spacers. At 25 C. the product is a clear, viscous or plastic, semi-solid material.
In the drawing is shown a typical roll type of capacitor (condenser) consisting of aluminum armatures I, 2 and having terminals 3, 4 of the elongated strip type. Between adjacent turns of the armatures are porous spacers 5, 5' which are adapted to be impregnated with an electroapplied to the terminal plates or armatures.
lyte. In some cases the spacer may be omitted. When a spacer is desired it may consist of a fabric, such as cheesecloth, or of paper.
In the particular case illustrated, the spacer consists of paper, which may be .001" in thickness and be sufficiently absorbent to be capable of being impregnated by the electrolyte when the latter is heated to 90 C. to 100 C. or thereabouts. Although but one sheet of paper is shown between adjacent turns, two or three may be used. As used in Fig. 2, capacitor armatures G, i may be stacked superposed, instead of rolled, preferably with one or more interposed spacers, one of which is indicated at 8. Terminals 9, ID are The aluminum foil should be treated to form an oxygenous film thereon prior to assembling of the capacitor parts, preferably by electrolytic treatment as described in prior Clark and Koenig Patent No. 2,022,500, patented November 26, 1935.
The impregnation of a capacitor unit consisting of aluminum foil armatures with or without spacers therebetween when properly assembled may be carried out by immersing the unit in an electrolyte composition made as herein described while the latter is heated to a temperature at which it is thinly liquid, for example 100 C. Preferably gas under pressure of about 100 lbs. per square inch is applied to insure penetration of the electrolyte into the interstices oi the unit. The impregnated capacitor may be cured in accordance with the usual methods, for example, by applying intermittent uni-directional voltage of alternating polarity followed by the application of intermittent alternating voltage of no volts-60 cycles.
Capacitors thus fabricated have a power factor of approximately 7% at 25 C., the capacity being about one microfarad for nine square inches oi active foil surface. When capacitors so fabricated are subjected to temperatures as th gh as 75 C. even for a period of several weeks, no deterioration occurs in the capacity characteristic and in fact an improvement may resilit.
Example 2 In some cases it is desirable to treat an elec= trolyte made as above described and containing 25% formamide with ammonia gas in order to produce a substantially neutral condition. For example, if the pyrogenous product is'treated with ammonia gas until the pill value is about 6.8 to 7, the resulting product consists oi. a thin, clear liquid at 90 C. and solidifies to a clear yellow jelly at 25 C. The ammonia-treated product has a resistance at 90 C. of the order 125 to 150 ohms/cm and at 25 C. of the order of soot ohms/ch1 It will be observed that the treatment with ammonia reduces the resistance value. While the treatment with ammonia does not appreciably change the capacity characteristic of capacitor units impregnated with such product, the power factor is found to be reduced, being as low as 5% at 25 C. subjection of units impregnated with this product to temperatures of 75 C. results in an improvement. In any event no deterioration results due to heating.
Example 3 In some cases it is desirable to mix the ingredients, namely, lactic acid, boric acid and formamide before being subjected to heat treatment. A mixture consisting by weight of 48% lactic acid, 27% boric acid and 25% formamide is treated with ammonia gas at a temperature of 75 to C. until the pH value is of the order of 7.0 to 7.5. The product is heated at a temperature within'the range of about 130 to 140 C. for approximately 3 to 4 hours, or until the resistance of the pyrogenous product has reached a value of about 137 ohms/cm at C. The pyrogenous product is characterized in general by the properties already described in connection with the foregoing examples.
Example 4 In some instances the individual reagents may be prepared separately and then mixed thoroughly to obtain the desired electrolyte. For example, lactic acid may be treated with ammonia thereby forming ammonium lactate which then is heated to form a semi-solid lactamidecontaining product. This pyrogenous composition is admixed with ammonium borate crystals and formamide in the proportions above indicated. The resulting product is heated to a temperature at which it is liquid and impregnation is carried out as above described.
While the proportions given in connection with the above examples are to be considered illustrative only, in general it is preferred that the amide which may consist oi. formamide, or a combination of amides such as acetamide and formamide, should not constitute more than 40% by weight of the total mixture. Itis also preferred in general that the lactic acid component of the final product should be at least as great as the amide component. In place of lactic acid, other aliphatic hydroxy acids may be used, such as heretofore indicated.
In place of the ammonium borate salts of other oxygen-containing acids may be used as ionogens. as, for example, the ammonium or alkali salts (sodium or potassium salts) of phosphoric acid, tartaric acid, acetic acid or citric acid.
Wherever in the accompanying claims specific reference is made to formamide, it is to be understooolthat equivalent amides, as, for example, acetamide, are included in the scope of such claims.
What we claim as new and desire to secure by Letters Patent of the United States is:
i. A resinous product derived by the heat treatrnent of a mixture oi lactic acid and ammonium lactate, said product being a waxy solid at 25 C. and a clear liquid at 90 C.
2. A viscous, semi-solid impregnating composition for electrolytic capacitors having filmiorn'iing electrodes, said impregnant including ammonium borate, a waxy solid product derived by heat treatment of ammoniated lactic acid, constituting a major ingredient and iormamide, constituting a minor ingredient, said composition being liquid at 90 C.
3. The process of preparing a composition adapted for impregnating capacitors which consists in combining ammonia with a mixture comprising a major proportion of lactic acid and a minor proportion of boric acid to form a liquid product, heating said product to a temperature of about to C. for several hours, and compounding the resulting product with a saturated, aliphatie, monoprimary amide.
a. The process of preparing an electrolyte composition which consists in forming a mixture of about 64 per cent lactic acid and 36 per cent boric acid, conducting ammonia into said mixture to form the corresponding ammonium compounds from said acids, heating the resulting .material and an inner ester derived by heating to a temperature of at least about C. a mixture of an acid of the group consisting of alpha, gamma and delta monobasic, saturated hydroxy aliphatic acid and ammonium salt of an acid of said group.
6. The combination of film-forming electrodes and a composition comprising the combination of an ionogen, iormamide and a product derived by heating to a temperature of at least about 120 C. a mixture of an acid of said group consisting of alpha, gamma and delta monobasic, saturated hydroxy aliphatic acid and ammonium salt of an acid of said group.
7. A composition comprising in combination a waxy product derived by heating ammoniated lactic acid to about 120 to C., an ionogen, and a resistance-reducing material.
8. A composition comprising a mixture of a waxy product derived by heating lacticacid to at least about 120 C., an ionogen, and formamide in a quantity suficient to appreciably modify the electric resistivity of said mixture.
9. A semi-solid balsamic materiai for use with film-forming electrodes comprising the combination of an ionogen, saturated, monoprimary organic amide and a waxy product derived by heating an ammoniated compound of lactic acid.
10. A resinous product derived by the prolonged heat treatment at about 120 to C. of an acid of the group consisting of the alpha, gamma and delta monobasic, saturated hydroxy aliphatic acids and an ammonium salt of an acid of such group.
11. An electric capacitor containing film-forming armatures and an electrolyte comprising the combintion of an ionogen, iormamide and a product derived by heating to a temperature of about 120 to 140 C. for several hours an ammoniated acid of the group consisting of alpha, gamma and delta monobasic, saturated hydroxy aliphatic acid.
12. A composition of matter comprising the combination of .an ionogen, a saturated, monoprimary organic amide, and an inner ester derived by heating to a temperature of about 120 to 140 0., an ammoniated, saturated hydroxy aliphatic acid.
FRANK M. CLARK. RALPH A. RUSCETTA.
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US69405A US2165090A (en) | 1936-03-17 | 1936-03-17 | Resinous compositions and capacitors containing the same |
FR816058D FR816058A (en) | 1936-01-07 | 1937-01-07 | Electrolytic capacitors and new electrolytes, specially adapted for their manufacture |
BE422118D BE422118A (en) | 1936-01-07 | 1937-06-16 | |
BE435689D BE435689A (en) | 1936-01-07 | 1939-07-28 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US69405A US2165090A (en) | 1936-03-17 | 1936-03-17 | Resinous compositions and capacitors containing the same |
Publications (1)
Publication Number | Publication Date |
---|---|
US2165090A true US2165090A (en) | 1939-07-04 |
Family
ID=22088763
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US69405A Expired - Lifetime US2165090A (en) | 1936-01-07 | 1936-03-17 | Resinous compositions and capacitors containing the same |
Country Status (1)
Country | Link |
---|---|
US (1) | US2165090A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2443843A (en) * | 1944-03-13 | 1948-06-22 | Distillers Co Yeast Ltd | Glycerol substitutes |
US2934682A (en) * | 1956-07-05 | 1960-04-26 | Sprague Electric Co | Electrolytes |
US2965816A (en) * | 1956-04-03 | 1960-12-20 | Sprague Electric Co | Electrolytic capacitor |
US3001108A (en) * | 1958-12-19 | 1961-09-19 | Gen Electric | Electrolytic capacitor and electrolyte therefor |
US3231792A (en) * | 1962-10-18 | 1966-01-25 | Sprague Electric Co | Electrolytic capacitor |
-
1936
- 1936-03-17 US US69405A patent/US2165090A/en not_active Expired - Lifetime
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2443843A (en) * | 1944-03-13 | 1948-06-22 | Distillers Co Yeast Ltd | Glycerol substitutes |
US2965816A (en) * | 1956-04-03 | 1960-12-20 | Sprague Electric Co | Electrolytic capacitor |
US2934682A (en) * | 1956-07-05 | 1960-04-26 | Sprague Electric Co | Electrolytes |
US3001108A (en) * | 1958-12-19 | 1961-09-19 | Gen Electric | Electrolytic capacitor and electrolyte therefor |
US3231792A (en) * | 1962-10-18 | 1966-01-25 | Sprague Electric Co | Electrolytic capacitor |
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